Amphiphilic peptide matrices for treatment of osteoporosis

Abstract

The present invention provides methods for prevention, prevention of progression, and treatment of osteoporosis and pre-osteoporotic conditions comprising direct administering to osteoporotic bone of a composition comprising amphiphilic peptides and peptide matrices thereof, useful in promoting biomineralization, local osteoporotic medications and inducing bone repair.

Description

[0001]This application is a division of U.S. patent application Ser. No. 12 / 746,168 filed Aug. 11, 2010, now U.S. Pat. No. 9,457,056, which is a 371 filing of International patent application no. PCT / IL2008 / 001570 filed Dec. 3, 2008, which claims the benefit of U.S. provisional patent application No. 60 / 992,109 filed Dec. 4, 2007, the entire contents of each of which are incorporated herein by reference thereto.FIELD OF THE INVENTION[0002]The present invention relates to therapeutic methods for treatment and prevention of progression of osteoporosis and related conditions by direct, local or intralesional administration, to the bone, of compositions comprising amphiphilic peptides and hydrogel matrices formed by these peptides.BACKGROUND OF THE INVENTION[0003]Osteoporosis[0004]Osteoporosis is defined as a disease characterized by low bone mass and microarchitecture deterioration of bone tissue, leading to enhanced bone fragility and a consequent increase in fracture risk. The most f...

AI Technical Summary

Benefits of technology

The present invention is about using certain peptides to treat and prevent bone defects associated with osteoporotic conditions. These peptides can be administered directly to the bone and are safe, non-immunogenic, and biodegradable. The peptides form scaffolds for mineralization and can be used as carriers for bioactive agents such as growth factors and antioxidants. The peptides can also be mixed or linked together to create matrices for bone regeneration. The invention also includes methods for preventing and treating bone fractures and weakened bones. The peptides can be injected as a viscous cement to fill voids in bones. Overall, the invention provides pharmaceutical compositions to enhance bone repair and strengthen bones.

Problems solved by technology

Osteoporosis is defined as a disease characterized by low bone mass and microarchitecture deterioration of bone tissue, leading to enhanced bone fragility and a consequent increase in fracture risk.

Osteoporotic vertebral fractures are associated with a significant increase in morbidity and mortality including severe and chronic back pain, functional limitation, height loss, spinal deformity, and disability.

The method produces an in situ polymerization and gives immediate results on bone pain.

PMMA has some disadvantages including excess heat generated during the polymerization process, and the possibility of inducing giant cell granulomas and fibrous reactions.

Adjacent vertebral overload has been reported with maximal PMMA filling, possibly provoking fractures.

This treatment reduces the risk of cement migration, yet it suffers other limitations as poor contact between the filler and the bone tissue.

Composite cements containing methacrylic polymers and HA have been proposed but all these biomaterials are not resorbable or biodegradable.

Treatment of vertebroplasty using calcium phosphate cement (CPC) alone in such patients has been reported, but complications such as recrushing of the vertebra and prolapse of the cement into the spinal canal may occur.

The retention of bone by inhibition of bone turnover may not be sufficient protection against fracture risk for patients who already have significant bone loss.

Thus, bisphosphonates seem to be non-biodegradable, both in animals and in solution.

Alendronate has also been shown to cause erosions and ulcers in the human stomach and to interfere with the healing of pre-existing lesions when given to healthy volunteers at doses that are prescribed for the treatment of osteoporosis and Pagets disease of bone.

Inorganic materials such as calcium phosphate and hydroxyapatite have been utilized as bone and dental fillers (reviewed in LeGeros, 2002) but lacking many of the extra cellular like functionalities, none can be considered entirely satisfactory in meeting the criteria required for successful tissue engineering.

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